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rs141724500

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs141724500(G;T)
Make rs141724500(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position33438897
GeneSNTA1
is asnp
is mentioned by
dbSNPrs141724500
ebirs141724500
HLIrs141724500
Exacrs141724500
Varsomers141724500
Maprs141724500
PheGenIrs141724500
hapmaprs141724500
1000 genomesrs141724500
hgdprs141724500
ensemblrs141724500
gopubmedrs141724500
geneviewrs141724500
scholarrs141724500
googlers141724500
pharmgkbrs141724500
gwascentralrs141724500
openSNPrs141724500
23andMers141724500
23andMe allrs141724500
SNP Nexus

SNPshotrs141724500
SNPdbers141724500
MSV3drs141724500
GWAS Ctlgrs141724500
Max Magnitude0
ClinVar
Risk rs141724500(A,T;A,T)
Alt rs141724500(A,T;A,T)
Reference rs141724500(G;G)
Significance Probable-Pathogenic
Disease not provided not specified
Variation info
Gene SNTA1
CLNDBN not provided not specified
Reversed 0
HGVS NC_000020.10:g.32026703G>T
CLNSRC
CLNACC RCV000171113.3, RCV000185527.2,